JPH10212489A - Cleanser composition - Google Patents

Cleanser composition

Info

Publication number
JPH10212489A
JPH10212489A JP3330297A JP3330297A JPH10212489A JP H10212489 A JPH10212489 A JP H10212489A JP 3330297 A JP3330297 A JP 3330297A JP 3330297 A JP3330297 A JP 3330297A JP H10212489 A JPH10212489 A JP H10212489A
Authority
JP
Japan
Prior art keywords
group
bis
microbicide
present
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP3330297A
Other languages
Japanese (ja)
Inventor
Kazuyuki Tsubone
和幸 坪根
Fumiichi Okabe
文市 岡部
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kanebo Ltd
Original Assignee
Kanebo Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kanebo Ltd filed Critical Kanebo Ltd
Priority to JP3330297A priority Critical patent/JPH10212489A/en
Publication of JPH10212489A publication Critical patent/JPH10212489A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain a cleanser composition including a stably formulated microbicide and capable of imparting effects for sufficiently preventing itching, and deodorant or odor-removing effects to a scalp, also excellent in detergency and foaming ability and useful as a cleansing cream, etc., by including prescribed amounts of a specific anionic surfactant and the microbicide. SOLUTION: This cleansing composition comprises (A) one or not less than two kinds of anionic surfactants with two chains and two polar groups containing amido groups e.g. N,N'-bis[2-myristoylamidoethyl]ethylenediamine-N, N'-di(sodium acetate)}, (B) 0.002-5wt.% microbicide of one or more compounds selected from a group of 2,4,4'-trichloro-2-hydroxydiphenyl ether, 3,4,4'- trichlorocarbanilide, benzethonium chloride, zinc bis(2-pyridylthio)-N-oxide, piroctoneolamin, photosensitive materials, an 8-22C unsaturated fatty acid such as undecylenic acid and sulfur, and preferably (C) 1-40wt.% clay mineral.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、殺菌効果を十分に
発揮するために頭皮に十分な痒み防止性、防臭・消臭効
果を付与でき、洗浄力、起泡力にもすぐれる洗浄剤組成
物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a detergent composition capable of imparting sufficient antipruritic, deodorizing and deodorizing effects to the scalp in order to sufficiently exert a bactericidal effect, and having excellent detergency and foaming power. About things.

【0002】[0002]

【従来の技術】消費者ニーズの多様化に伴い、殺菌効果
を有する洗浄剤組成物が多く検討されている。洗浄剤組
成物に主要成分として含有される陰イオン界面活性剤は
陽イオン性殺菌剤と錯体を形成するために、殺菌効果が
十分に発揮されない場合が多い。また、一般に、洗浄剤
組成物に含まれる塩素系殺菌剤は、長期間の貯蔵又は保
管によって殺菌効果が低下することが知られている。洗
浄剤組成物に配合されている殺菌剤の効果を損なうこと
なく洗浄剤組成物の変質を防ぐために、通常、抗酸化
剤、金属封鎖剤、粘土鉱物などの安定化剤が洗浄剤組成
物に配合される。しかし、これらの安定化剤を配合した
洗浄剤組成物(例えば、特公平7−53657号公報、
特開平8−109394号公報)は、殺菌効果の低下を
抑制し、ある程度の殺菌効果を示すが、必ずしも十分で
はなく、洗浄力及び起泡力も十分に満足できるものでは
なかった。
2. Description of the Related Art With the diversification of consumer needs, many detergent compositions having a bactericidal effect have been studied. The anionic surfactant contained as a main component in the detergent composition forms a complex with the cationic germicide, and thus often does not sufficiently exert a bactericidal effect. In addition, it is generally known that a chlorine-based germicide contained in a detergent composition has a reduced bactericidal effect due to long-term storage or storage. In order to prevent deterioration of the detergent composition without impairing the effect of the bactericide contained in the detergent composition, a stabilizer such as an antioxidant, a sequestering agent, or a clay mineral is usually added to the detergent composition. Be blended. However, a detergent composition containing these stabilizers (for example, JP-B-7-53657,
Japanese Patent Application Laid-Open No. 8-109394) suppresses a decrease in the bactericidal effect and exhibits a certain bactericidal effect, but it is not always sufficient, and the cleaning power and the foaming power are not sufficiently satisfactory.

【0003】[0003]

【発明が解決しようとする課題】すなわち、本発明の目
的は、殺菌剤を安定に配合でき、高い殺菌効果を有する
結果、頭皮に十分な痒み防止性、防臭・消臭効果を付与
でき、洗浄力、起泡力にもすぐれる洗浄剤組成物を提供
するにある。
That is, an object of the present invention is to stably blend a bactericide and to have a high bactericidal effect, and thus to provide sufficient itch prevention, deodorant and deodorant effects to the scalp, and An object of the present invention is to provide a detergent composition having excellent power and foaming power.

【0004】[0004]

【課題を解決するための手段】かかる目的のもとで本発
明者は鋭意検討を行った結果、特定の陰イオン界面活性
剤と殺菌剤を含有する洗浄剤組成物が高い殺菌効果を有
するとともに、洗浄力、起泡力にもすぐれること、ま
た、それらの原材料に加えて粘土鉱物をさらに配合する
と殺菌効果が格段にすぐれることを見出し、本発明を完
成した。すなわち、本発明の請求項1の発明は、(A)
アミド基含有2鎖2極性基含有陰イオン界面活性剤の1
種又は2種以上と、(B)殺菌剤0.002〜5重量%
とを含有することを特徴とする洗浄剤組成物である。ま
た、本発明の請求項2の発明は、(A)アミド基含有2
鎖2極性基含有陰イオン界面活性剤の1種又は2種以上
と、(B)殺菌剤と,(C)粘土鉱物を含有することを
特徴とする洗浄剤組成物である。
Means for Solving the Problems Under such an object, the present inventors have conducted intensive studies and as a result, it has been found that a detergent composition containing a specific anionic surfactant and a bactericide has a high bactericidal effect and The present invention was found to be excellent in detergency, defoaming power, and foaming power, and that the bactericidal effect was remarkably improved when clay minerals were further added to these raw materials. That is, the invention of claim 1 of the present invention provides (A)
One of anionic surfactants containing an amide group-containing two-chain dipolar group
Seed or two or more, and (B) a fungicide 0.002 to 5% by weight
And a cleaning composition comprising: Further, the invention of claim 2 of the present invention provides (A) an amide group-containing 2
A cleaning composition comprising one or more anionic surfactants having a chain dipolar group, (B) a disinfectant, and (C) a clay mineral.

【0005】[0005]

【発明の実施の形態】次に本発明の実施の形態を説明す
る。本発明における(A)成分のアミド基含有2鎖2極
性基含有陰イオン界面活性剤は、長鎖疎水基の炭素数が
18、16、14、12、10又は8であり、極性基が
カルボキシル基、スルホン酸基、硫酸基のいずれかを持
ち、連結基が2〜6のアルキレン鎖を持つものである。
例示するとN,N’−ビス〔2−ラウラミドエチル)エ
チレンジアミン−N,N’−ジ(酢酸ナトリウム)が挙
げられる。この化合物の分子構造において疎水基の異な
る同族体との混合体としても本発明の目的の範囲内で配
合される。ここで用いる対イオンとしては1価又は2価
のアルカリ金属イオン、アンモニウムイオン又は有機ア
ンモニウムイオンが適用される。ただし、有機アンモニ
ウムイオンとしては、リジン、アルギニン等の塩基性ア
ミノ酸も該当する。N,N’−ビス〔2−ラウラミドエ
チル)エチレンジアミン−N,N’−ジ(酢酸ナトリウ
ム)の他、さらに具体的に例示すると、、N,N’−ビ
ス〔2−ミリストイラミドエチル)エチレンジアミン−
N,N’−ジ(酢酸ナトリウム)、N,N’−ビス〔2
−パルミトイラミドエチル)エチレンジアミン−N,
N’−ジ(酢酸ナトリウム)、N,N’−ビス〔2−ラ
ウラミドエチル)エチレンジアミン−N,N’−ジ(プ
ロピオン酸ナトリウム)、N,N’−ビス〔2−ミリス
トイラミドエチル)エチレンジアミン−N,N’−ジ
(プロピオン酸ナトリウム)、N,N’−ビス〔2−パ
ルミトイラミドエチル)エチレンジアミン−N,N’−
ジ(プロピオン酸ナトリウム)、N,N’−ビス(ラウ
ロイルアミド)エタン−N,N’−ジ(酢酸ナトリウ
ム)、N,N’−ビス(ミリストイルアミド)エタン−
N,N’−ジ(酢酸ナトリウム)、N,N’−ビス(パ
ルミトイルアミド)エタン−N,N’−ジ(酢酸ナトリ
ウム)、N,N’−ビス(ラウロイルアミド)エタン−
N,N’−ジ(プロピオン酸ナトリウム)、N,N’−
ビス(ミリストイルアミド)エタン−N,N’−ジ(プ
ロピオン酸ナトリウム)、N,N’−ビス(パルミトイ
ルアミド)エタン−N,N’−ジ(プロピオン酸ナトリ
ウム)、N,N’−ビス(ラウロイルアミド)ブタン−
N,N’−ジ(酢酸カリウム)、N,N’−ビス(ミリ
ストイルアミド)ブタン−N,N’−ジ(酢酸カリウ
ム)、N,N’−ビス(パルミトイルアミド)ブタン−
N,N’−ジ(酢酸カリウム)、N,N’−ビス(ラウ
ロイルアミド)エタン−N,N’−ジ(エタンスルホン
酸カリウム)、N,N’−ビス(ミリストイルアミド)
ブタン−N,N’−ジ(エタンスルホン酸カリウム)、
N,N’−ビス(パルミトイルアミド)エタン−N,
N’−ジ(エタンスルホン酸ナトリウム)が挙げられ
る。本発明において適用される2鎖2極性基含有陰イオ
ン界面活性剤は、2つの疎水基中にアミド基を含むもの
であり、その疎水基の炭素数は12又は14が起泡性の
点で最も好ましい。連結基としてのアルキレン鎖長は2
〜6が適用されるが、界面活性能の点で2が最も好まし
い。本発明において適用される2鎖2極性基含有陰イオ
ン界面活性剤の構造基であるカルボキシル基、硫酸基、
スルホン酸基、またはリン酸基という種類の中で皮膚刺
激性と界面活性能の点からカルボキシル基、スルホン酸
基が好ましい。これらの1種又は2種以上を用いる。配
合量は、剤型によって異なるが、通常、10〜50重量
%である。
Next, an embodiment of the present invention will be described. The amide group-containing two-chain bipolar group-containing anionic surfactant of the component (A) in the present invention has a long-chain hydrophobic group having 18, 16, 14, 12, 10 or 8 carbon atoms, and the polar group has a carboxyl group. Group, a sulfonic acid group or a sulfate group, and the linking group has 2 to 6 alkylene chains.
As an example, N, N'-bis [2-lauramidoethyl) ethylenediamine-N, N'-di (sodium acetate) can be mentioned. A mixture with a homologue having a different hydrophobic group in the molecular structure of the compound is also blended within the scope of the present invention. As the counter ion used here, a monovalent or divalent alkali metal ion, ammonium ion or organic ammonium ion is applied. However, basic amino acids such as lysine and arginine also correspond to the organic ammonium ion. In addition to N, N'-bis [2-lauramidoethyl) ethylenediamine-N, N'-di (sodium acetate), more specifically, for example, N, N'-bis [2-myristoamilamidoethyl) Ethylenediamine-
N, N'-di (sodium acetate), N, N'-bis [2
-Palmitoiramidoethyl) ethylenediamine-N,
N'-di (sodium acetate), N, N'-bis [2-lauramidoethyl) ethylenediamine-N, N'-di (sodium propionate), N, N'-bis [2-myristoylamidoethyl) Ethylenediamine-N, N'-di (sodium propionate), N, N'-bis [2-palmitoiramidoethyl) ethylenediamine-N, N'-
Di (sodium propionate), N, N'-bis (lauroylamide) ethane-N, N'-di (sodium acetate), N, N'-bis (myristoylamide) ethane-
N, N'-di (sodium acetate), N, N'-bis (palmitoylamide) ethane-N, N'-di (sodium acetate), N, N'-bis (lauroylamide) ethane-
N, N'-di (sodium propionate), N, N'-
Bis (myristoylamide) ethane-N, N′-di (sodium propionate), N, N′-bis (palmitoylamido) ethane-N, N′-di (sodium propionate), N, N′-bis ( Lauroylamide) butane-
N, N'-di (potassium acetate), N, N'-bis (myristoylamide) butane-N, N'-di (potassium acetate), N, N'-bis (palmitoylamide) butane-
N, N'-di (potassium acetate), N, N'-bis (lauroylamide) ethane-N, N'-di (potassium ethanesulfonate), N, N'-bis (myristoylamide)
Butane-N, N′-di (potassium ethanesulfonate),
N, N'-bis (palmitoylamide) ethane-N,
N′-di (sodium ethanesulfonate). The two-chain dipolar group-containing anionic surfactant applied in the present invention contains an amide group in two hydrophobic groups, and the hydrophobic group has 12 or 14 carbon atoms in terms of foaming property. Most preferred. The alkylene chain length as a linking group is 2
-6 are applied, but 2 is most preferable in terms of surface activity. Carboxyl group, sulfate group, which is a structural group of the two-chain dipolar group-containing anionic surfactant applied in the present invention,
Among the sulfonic acid groups or phosphoric acid groups, carboxyl groups and sulfonic acid groups are preferred from the viewpoints of skin irritation and surface activity. One or two or more of these are used. The compounding amount varies depending on the dosage form, but is usually 10 to 50% by weight.

【0006】本発明における(B)成分の殺菌剤として
は、洗浄剤組成物に汎用される殺菌剤が使用できるが、
2,4,4’−トリクロロ−2−ヒドロキシジフェニル
エーテル(以下、DP−300と略記する)、3,4,
4’−トリクロロカルバニリド(以下、TCCと略記す
る)、ベンゼトニウムクロリド、ジンクビス(2−ピリ
ジルシオ)−N−オキシド、ピロクトンオラミン、感光
素類、ウンデシレン酸などの炭素原子数8〜22の不飽
和脂肪酸、イオウが好ましい。特に、DP−300、T
CC及びベンゼトニウムクロリドが好ましい。殺菌剤
は、これらの化合物の1種又はそれ以上を組成物全量に
対して0.002〜5重量%、好ましくは0.05〜1
重量%の範囲内で使用する。
As the bactericide of the component (B) in the present invention, a bactericide commonly used in detergent compositions can be used.
2,4,4'-trichloro-2-hydroxydiphenyl ether (hereinafter abbreviated as DP-300), 3,4
4'-trichlorocarbanilide (hereinafter abbreviated as TCC), benzethonium chloride, zinc bis (2-pyridylsio) -N-oxide, pyrocton olamine, photosensitizers, undecylenic acid, etc., having 8 to 22 carbon atoms. Unsaturated fatty acids and sulfur are preferred. In particular, DP-300, T
CC and benzethonium chloride are preferred. The fungicide contains one or more of these compounds in an amount of 0.002 to 5% by weight, preferably 0.05 to 1% by weight based on the total weight of the composition.
Use within the range of weight%.

【0007】本発明における(C)成分の粘土鉱物は、
二酸化珪素を基本とする層状構造を有し、粒径が50μ
m以下、好ましくは0.05〜30μm範囲の微細な結
晶又はコロイド的性質を有する粒子である。代表的な粘
土鉱物としては、カオリナイト、雲母、タルク、モンモ
リオナイトなどがあり、好ましくはカオリナイトが挙げ
られる。これらの1種又はそれ以上を組成物全量に対し
て1〜40重量%を含有させる。
[0007] The clay mineral of the component (C) in the present invention is:
Has a layered structure based on silicon dioxide, with a particle size of 50μ
m or less, preferably particles having fine crystalline or colloidal properties in the range of 0.05 to 30 μm. Representative clay minerals include kaolinite, mica, talc, montmorillonite and the like, preferably kaolinite. One or more of these are contained in an amount of 1 to 40% by weight based on the total amount of the composition.

【0008】本発明の洗浄剤組成物は上記の如くの組成
からなるが、必要に応じて他の界面活性剤、乳化助剤、
香料、着色剤、防腐剤、保湿剤、顔料等を本発明の目的
を達成する範囲内で適宜配合することもできる。本発明
の洗浄剤組成物は、特定の陰イオン界面活性剤、粘土鉱
物を含有する固形、クリーム状又は液状の洗浄剤組成物
であり、洗顔クリーム、液状洗顔料、ボディシャンプ
ー、シャンプー等の皮膚又は頭皮の洗浄を目的とするも
のに適用される。
[0008] The cleaning composition of the present invention has the composition as described above. If necessary, other surfactants, emulsifying auxiliaries,
A fragrance, a colorant, a preservative, a humectant, a pigment and the like can be appropriately compounded within a range that achieves the object of the present invention. The cleansing composition of the present invention is a solid, creamy or liquid cleansing composition containing a specific anionic surfactant and a clay mineral, such as a face wash cream, a liquid facial cleanser, a body shampoo, a shampoo and the like. Or it is applied to the purpose of cleaning the scalp.

【0009】[0009]

【実施例】以下、実施例にて本発明を説明するが、本発
明はこの実施例によって限定されない。なお、配合量は
重量%である。 (1)抗フケ性、防臭性の評価 専門パネラー10名により、毎日1回、2週間、各シャ
ンプーを使用したときの抗フケ性、防臭性の効果を以下
の基準で評価した。 ◎:9名以上がフケが減少し、防臭性を認めると感じ
た。 ○:8名がフケが減少し、防臭性を認めると感じた。 △:7名がフケが減少し、防臭性を認めると感じた。 ×:6名以下がフケが減少し、防臭性を認めると感じ
た。 (2)洗浄性 健康な日本人女性の毛髪20g(15cm)にシャンプ
ー液1gを塗布し、1分間洗浄し、すすいだ後の感触を
専門パネラー20名により、以下の基準で評価した。 ◎:極めて良好(90%以上の人が洗浄力良好と答え
た) ○:良好(80〜90%未満の人が洗浄力良好と答え
た) △:若干不良(70〜80%未満の人が洗浄力良好と答
えた) ×:不良(70%未満の人が洗浄力良好と答えた) (3)起泡性 シャンプー液の20倍希釈水溶液50ミリリットル(2
0度C)を200ミリリットル容の共栓つきメスシリン
ダーにとり、1分間に100回震盪した後、直後の泡立
ち(泡高さ)を調べ、以下の基準で評価した。 ◎:極めて良好な泡立ち ○:良好な泡立ち △:泡立つが不十分 ×:泡立たない
EXAMPLES The present invention will be described below with reference to examples, but the present invention is not limited to these examples. In addition, the compounding amount is weight%. (1) Evaluation of anti-dandruff property and deodorant property The effect of anti-dandruff property and deodorant property when each shampoo was used once a day for two weeks by 10 expert panelists was evaluated according to the following criteria. :: 9 or more felt that dandruff was reduced and deodorization was recognized. :: Eight people felt that dandruff was reduced and deodorization was recognized. Δ: Seven people felt that dandruff was reduced and that deodorization was recognized. ×: Six or less felt that dandruff was reduced and deodorization was recognized. (2) Detergency 1 g of a shampoo solution was applied to 20 g (15 cm) of hair of a healthy Japanese woman, washed for 1 minute, and the feel after rinsing was evaluated by 20 expert panelists according to the following criteria. ◎: extremely good (more than 90% of the people answered that the cleaning power is good) ○: good (more than 80 to 90% of the people answered that the cleaning power was good) △: slightly poor (more than 70 to 80% of the people ×: poor (less than 70% of people answered that cleaning power was good) (3) Foaming property 50 ml of 20-fold diluted aqueous solution of shampoo solution (2
0 ° C) was placed in a 200-ml graduated cylinder equipped with a stopper and shaken 100 times a minute, immediately after which foaming (bubble height) was examined and evaluated according to the following criteria. ◎: extremely good foaming ○: good foaming Δ: foaming is insufficient x: no foaming

【0010】実施例1〜18,比較例1〜12 表1〜3に本発明の洗浄剤組成物(試験試料)の組成を
示す。ここに示す配合物は次のものを示す。 (1)配合される(A)成分のアミド基含有2鎖2極性
基含有陰イオン界面活性剤 A1:N,N’−ビス(ラウロイルアミド)エタン−
N,N’−ジ(酢酸ナトリウム) A2:ラウリルエーテル硫酸ナトリウム(対照化合物) (2)配合される(B)成分の殺菌剤 B1:DP−300(2,4,4’−トリクロロ−2−
ヒドロキシジフェニルエーテル) B2:TCC(3,4,4’−トリクロロカルバニリ
ド) B3:塩化ベンゼトニウム (3)配合される(C)成分の粘土鉱物 C1:カオリン C2:タルク
Examples 1 to 18 and Comparative Examples 1 to 12 Tables 1 to 3 show the compositions of the cleaning compositions (test samples) of the present invention. The formulations shown here show the following: (1) An amide group-containing two-chain bipolar group-containing anionic surfactant of the component (A) to be blended A1: N, N'-bis (lauroylamide) ethane-
N, N'-di (sodium acetate) A2: sodium lauryl ether sulfate (control compound) (2) Bactericide of component (B) to be blended B1: DP-300 (2,4,4'-trichloro-2-)
(Hydroxydiphenyl ether) B2: TCC (3,4,4'-trichlorocarbanilide) B3: benzethonium chloride (3) Clay mineral of component (C) blended C1: kaolin C2: talc

【0011】[0011]

【表1】 [Table 1]

【0012】[0012]

【表2】 [Table 2]

【0013】[0013]

【表3】 [Table 3]

【0014】表1〜3の結果から、本発明の洗浄剤組成
物を使って洗髪した場合は、前記評価項目のすべてです
ぐれていることがわかる。一方、本発明の洗浄剤組成物
の構成成分のうちいずれか一つが欠ける比較例の洗浄剤
組成物の性能は本発明の洗浄剤組成物のそれよりも大幅
に悪いことがわかる。
From the results in Tables 1 to 3, it can be seen that when the hair was washed using the cleaning composition of the present invention, all of the above evaluation items were excellent. On the other hand, it can be seen that the performance of the cleaning composition of the comparative example lacking any one of the components of the cleaning composition of the present invention is much worse than that of the cleaning composition of the present invention.

【0015】[0015]

【発明の効果】以上記載の如く、本発明は、殺菌効果を
十分に発揮するために頭皮に十分な痒み防止性、防臭・
消臭効果を付与できるとともに洗浄力、起泡力にすぐれ
る洗浄剤組成物を提供することは明らかである。
As described above, the present invention has sufficient anti-itch, anti-odor and scalp properties on the scalp in order to sufficiently exhibit a bactericidal effect.
It is apparent that the present invention provides a detergent composition which can impart a deodorizing effect and has excellent detergency and foaming power.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 (A)アミド基含有2鎖2極性基含有陰
イオン界面活性剤の1種又は2種以上と、(B)殺菌剤
0.002〜5重量%とを含有することを特徴とする洗
浄剤組成物。
1. A composition comprising (A) one or more amide group-containing two-chain bipolar group-containing anionic surfactants and (B) a bactericide in an amount of 0.002 to 5% by weight. The cleaning composition.
【請求項2】 (A)アミド基含有2鎖2極性基含有陰
イオン界面活性剤の1種又は2種以上と、(B)殺菌剤
0.002〜5重量%と,(C)粘土鉱物1〜40重量
%とを含有することを特徴とする洗浄剤組成物。
2. (A) one or more amide group-containing two-chain bipolar group-containing anionic surfactants, (B) a fungicide 0.002 to 5% by weight, and (C) a clay mineral A cleaning composition comprising 1 to 40% by weight.
【請求項3】 前記殺菌剤が、2,4,4’−トリクロ
ロ−2−ヒドロキシジフェニルエーテル、3,4,4’
−トリクロロカルバニリド、ベンゼトニウムクロリド、
ジンクビス(2−ピリジルシオ)−N−オキシド、ピロ
クトンオラミン、感光素類、ウンデシレン酸などの炭素
原子数8〜22の不飽和脂肪酸、イオウからなる群から
選択される1種又はそれ以上の化合物である請求項1又
は2に記載の洗浄剤組成物。
3. The bactericide is 2,4,4′-trichloro-2-hydroxydiphenyl ether, 3,4,4 ′.
-Trichlorocarbanilide, benzethonium chloride,
One or more compounds selected from the group consisting of unsaturated fatty acids having 8 to 22 carbon atoms, such as zinc bis (2-pyridylcio) -N-oxide, pyroctone olamine, photosensitizers, undecylenic acid, and sulfur The cleaning composition according to claim 1 or 2, wherein
JP3330297A 1997-01-30 1997-01-30 Cleanser composition Pending JPH10212489A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3330297A JPH10212489A (en) 1997-01-30 1997-01-30 Cleanser composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3330297A JPH10212489A (en) 1997-01-30 1997-01-30 Cleanser composition

Publications (1)

Publication Number Publication Date
JPH10212489A true JPH10212489A (en) 1998-08-11

Family

ID=12382764

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3330297A Pending JPH10212489A (en) 1997-01-30 1997-01-30 Cleanser composition

Country Status (1)

Country Link
JP (1) JPH10212489A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008139699A1 (en) 2007-04-27 2008-11-20 Mitsubishi Chemical Corporation Degradation odor-inhibiting agent and antibacterial agent
JP2011057979A (en) * 2009-08-13 2011-03-24 Lion Corp Detergent composition
US7977302B2 (en) 2005-12-07 2011-07-12 Conopco, Inc. Detergent bar composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7977302B2 (en) 2005-12-07 2011-07-12 Conopco, Inc. Detergent bar composition
WO2008139699A1 (en) 2007-04-27 2008-11-20 Mitsubishi Chemical Corporation Degradation odor-inhibiting agent and antibacterial agent
US8389029B2 (en) 2007-04-27 2013-03-05 Mitsubishi Chemical Corporation Deterioration smell inhibitor and antimicrobial
JP2011057979A (en) * 2009-08-13 2011-03-24 Lion Corp Detergent composition

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